A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919438



Internal ID22694660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135678137..135679899hg38UCSC Ensembl
chr7:135362885..135364647hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381763
hg191763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919438
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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